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TCI

CAS 7686-77-3

3-Cyclopentene-1-carboxylic Acid TCI C1914

3-Cyclopentene-1-carboxylic Acid TCI C1914

Chemical Identity

CAS No.
7686-77-3
PubChem
CID 853756·SID 87561547
Formula
C6H8O2
Molecular weight
112.13 g/mol
Purity
>97.0%(GC)(T)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
cyclopent-3-ene-1-carboxylic acid
SMILES
C1C=CCC1C(=O)O
InChIKey
XVSYDLITVYBCBD-UHFFFAOYSA-N
MDL
MDL00101764
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3-Cyclopentene-1-carboxylic Acid is a chemical compound widely used as a foundational building block in organic synthesis. Its unique molecular structure, featuring a cyclopentene ring connected to a carboxylic acid group, makes it a versatile reagent in laboratory settings. This compound is essential for the development of complex organic molecules, particularly in reactions involving substitution or addition mechanisms. Its role in creating heterocyclic compounds, esters, and other functional derivatives is critical in both academic and industrial research environments.

The compound's chemical properties make it a preferred choice for synthetic chemists. It exhibits stability under controlled conditions but is sensitive to oxidation and moisture, requiring careful handling. Its simple yet adaptable structure allows for a wide range of chemical modifications, making it suitable for high reactivity applications. The flexibility of its molecular framework enables it to participate in various reaction pathways, enhancing its utility in organic synthesis.

In Indonesian laboratories, 3-Cyclopentene-1-carboxylic Acid is commonly used by researchers, students, and pharmaceutical industries. It plays a vital role in the synthesis of bioactive compounds, drug development, and industrial chemical production. Its availability in the local market ensures accessibility for those requiring high-quality raw materials for their experiments and projects.

  • Organic synthesis of heterocyclic compounds due to its cyclopentene ring structure and carboxylic acid functionality.
  • Preparation of ester derivatives through esterification reactions with alcohols and acid catalysts.
  • Development of bioactive compounds in pharmaceutical research for drug discovery and formulation.
  • Industrial chemical production where functional group modification is required for polymer synthesis.
  • Research in chemical modification of organic molecules requiring high reactivity and structural versatility.

Brand TCI
CAS number 7686-77-3
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply
Physical form Solid or liquid, depending on supplier packaging
Storage Store in a cool, dry place away from moisture and oxidizing agents

This compound should be stored in a cool, dry environment to prevent degradation due to moisture and oxidation. It is recommended to use airtight containers made of glass or polyethylene to minimize exposure to air and humidity. Laboratory personnel should handle the material with care, using appropriate personal protective equipment such as gloves and safety goggles. Avoid contact with strong oxidizing agents to prevent unwanted reactions. Ensure proper ventilation in the workspace to reduce the risk of inhalation of any vapors. Regular monitoring of storage conditions is advised to maintain the compound's integrity and effectiveness for research applications.

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